Generation of CDMLe012-A-1 cells: A pluripotent human embryonic stem cell model of Turner's syndrome

Stem Cell Res. 2019 Aug:39:101508. doi: 10.1016/j.scr.2019.101508. Epub 2019 Jul 23.

Abstract

Monosomy of chromosome X is associated with high prenatal mortality of female embryos and severe developmental abnormalities of patients born with Turner's syndrome (45,XO). The CDMLe012-A-1 human embryonic stem cell (hESC) line, derived from a day six blastocyst with a normal 46,XX female karyotype spontaneously lost an X-chromosome during cell culture. This 45,XO karyotype was stably maintained for more than 55 passages. Since the CDMLe012-A-1 cells express pluripotent stem cell markers and differentiate into cells derived from the three germ layers, the cell line represents a stable, pluripotent stem cell model of Turner's syndrome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blastocyst / cytology
  • Blastocyst / metabolism
  • Cell Differentiation / genetics
  • Cell Differentiation / physiology
  • Female
  • Human Embryonic Stem Cells / cytology*
  • Human Embryonic Stem Cells / metabolism*
  • Humans
  • Karyotype
  • Karyotyping
  • Pregnancy
  • Turner Syndrome / genetics*